Job Description
📋 Description Lead QA activities for pharmacovigilance quality systems globally Audit programs across clinical safety and post-market PV Support inspections, CAPAs, change controls, and quality docs Provide QA guidance to cross-functional teams Monitor regulatory intelligence and evolving PV requirements Travel as needed, including occasional short-notice trips 🎯 Requirements Bachelor’s degree with 8+ years, Master’s 6+ years, or PhD 3+ years for Assistant Director; higher Experience in GVP QA, clinical safety, PV or related life sciences Strong PV audit experience (internal, partner, service provider) Knowledge of global PV regulations (FDA/EMA), ICH, GCP Experience with regulatory inspections and readiness Understanding of SOPs, CAPAs, deviations, change controls, QA docs 🎁 Benefits Competitive salary: Assistant Director $121,205 – $162,726; Associate Director $138,908 – $196,548 Fully remote work opportunity within the United States Comprehensive benefits package Opportunities to contribute to meaningful healthcare solutions Collaborative environment with cross-functional teams
